Sleep secrets for surgeons: could better rest boost performance after surgery?

NCT ID NCT06213246

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 24, 2026 · Last updated Aug 25, 2026 · Updated 1 time

Summary

This study looks at whether following simple sleep hygiene tips—like keeping a consistent schedule and a cool, quiet bedroom—can help orthopedic surgeons recover strength and mental sharpness after performing surgery. Researchers will measure handgrip strength, sleep quality, stress hormones, and cognitive performance before and after operations, comparing a normal week to a week with these sleep strategies. The goal is to see if these habits can reduce fatigue and improve recovery for surgeons.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Sleep hygiene strategies (behavioral guidelines for better sleep)
What this could lead to
If effective, these strategies could improve surgeons' recovery and performance, potentially enhancing patient safety and surgeon well-being.
What could go wrong
The trial is small (15 participants) and early, so results may not apply broadly. Also, sleep hygiene may not fully counteract the physical and mental demands of surgery.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

15 people

The number who actually took part.

Started

Oct 2023

Finished

Dec 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

23 to 70 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Male or female, of any ethnicity; * Age between 23 and 70 years old; * Cognitively intact; * Orthopedic surgeons or medical residents specializing in Orthopedics. * Signature and acceptance of informed consent to collaborate in all procedures necessary for the study. Exclusion Criteria: * Individuals younger than 23 years old or older than 70 years old; * Any clinical condition that prevents the subject from participating in operating room activities (e.g., muscle injury, COVID-19 positivity, feverish or flu-like states, etc.). * Non-participation, for any reason, in surgical activities in daily clinical practice. * Clinically diagnosed sleep disorders. * Women who have been pregnant or breastfeeding within 12 months before signing the informed consent or during the recruitment and observation period. \[self-declaration\] * Non-acceptance of the informed consent. * Physical impossibility to undergo the evaluations required by the study using the devices specified in the protocol.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • IRCCS Ospedale Galeazzi-Sant'Ambrogio

    Milan, Milan, Italy

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